You will be responsible in setting up trials, ensuring that trials run smoothly; this will include accurate record keeping and drug accountability of clinical trials, reviewing protocol specific guidelines and liaising within a multi-disciplinary team. You will need to be able to multitask, possess excellent communication skills, meet tight deadlines and thrive in a busy office. Your Responsibilities What youll do Support dispensing of clinical trials prescriptions Once ACPT qualified; support checking of clinical trials prescriptions Setup of assigned clinical trial studies Follow site procedure accurately of set up accurately and promptly Liaise with Clinical Research Associate/Organisation (CRA/CRO) to fulfil workflow tasks need for each assigned study in set up Following up in a timely manner on all queries with Clinical Research Associate/Organisation (CRA/CRO) Efficient production of study site file documentation What were looking for A strong team player. Friendly and approachable manner. Polite, sympathetic, patient and diplomatic Proven ability to work to deadlines, prioritise and multi-task Able to learn and assimilate complex information quickly.